Status: current, Primitive. Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5071675017 | Isolated hypoplasia of fovea centralis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
5071676016 | Isolated foveal hypoplasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
5071677013 | Isolated hypoplasia of fovea centralis | en | Synonym | Active | Case insensitive | SNOMED CT core |
5071678015 | A rare macular disorder with characteristics mostly of a variable degree of decreased visual acuity, jerk or pendular nystagmus and typical ocular findings at imaging. The disease is usually bilateral. Rarely nystagmus can be absent. Locally the disease has characteristics of an underdeveloped foveal pit, absence of foveal pigmentation and/or foveal avascular zone and persistence of inner retinal layers at the fovea in absence of concomitant ocular or systemic pathology. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Isolated foveal hypoplasia | Is a | Anomaly of eye | true | Inferred relationship | Some | ||
Isolated foveal hypoplasia | Is a | Disorder of macula of retina | true | Inferred relationship | Some | ||
Isolated foveal hypoplasia | Is a | Developmental disorder | true | Inferred relationship | Some | ||
Isolated foveal hypoplasia | Finding site | Structure of fovea centralis | true | Inferred relationship | Some | 1 | |
Isolated foveal hypoplasia | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Isolated foveal hypoplasia | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set